Oral-B Minute-Foam Banana Splitz

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Overview

What is Oral-B Minute-Foam Banana Splitz?

What does Oral-B Minute-Foam Banana Splitz look like?

What are the available doses of Oral-B Minute-Foam Banana Splitz?

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What should I talk to my health care provider before I take Oral-B Minute-Foam Banana Splitz?

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How should I use Oral-B Minute-Foam Banana Splitz?

DOSAGE AND ADMINISTRATION:

Adults and Children 6 years and over: Use foam 2 times a year.

This initial time you dispense from a new bottle, gently lift upward on the nozzle to break the protective seal (thin plastic located adjacent to trigger). If this seal is broken do not use the product. Shake bottle vigorously for 3-4 seconds prior to dispensing. Invert bottle 180 degree with nozzle tip pointed downward into tray. Place nozzle tip close to the tray floor and at one end of the tray arch. Moving from one end of the tray to the other in one fluid motion, slowly press down on the trigger. Dispense foam into applicator tray. (Note: foam will expand slightly to fill the tray.) Immediately place trays in mouth. (Do not fill trays with foam too far in advance of treatment as the foam will collapse and not be as effective.) Have patient bite down on the trays lightly but firmly for 4 minutes. Remove trays and have patient expectorate excess. Instruct patient not to eat, drink, or rinse for at least 30 minutes. For optimal tooth coverage, use a fluoride applicator tray which is deep enough to reach the entire vertical height of all teeth (even the molars)

What interacts with Oral-B Minute-Foam Banana Splitz?

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What are the warnings of Oral-B Minute-Foam Banana Splitz?

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What are the precautions of Oral-B Minute-Foam Banana Splitz?

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What are the side effects of Oral-B Minute-Foam Banana Splitz?

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What should I look out for while using Oral-B Minute-Foam Banana Splitz?

What might happen if I take too much Oral-B Minute-Foam Banana Splitz?

Accidental ingestion of large amounts of fluoride can result in acute irritation of the mouth and gastrointestinal symptoms such as nausea, vomiting, diarrhea, hematemesis epigastric cramping and abdominal pain. If large amounts of fluoride equal to or greater than 5mg fluoride/kg body weight (or 2.3 mg fluoride/lb body weight) are ingested, give calcium (e.g. milk, 5% calcium gluconate or calcium lactate solution) orally to relieve gastrointestinal symptoms and admit immediately to a hospital facility.

A standard treatment dose of Minute-Foam contains approximately 12.4 mg fluoride. One 165 g (5.8oz) bottle contains approximately 1.95 g of fluoride.

How should I store and handle Oral-B Minute-Foam Banana Splitz?

Store at controlled room temperature 20-25C (68-77F). Excursions permitted to 15-30C (59-86F). [See current USP]Dispense in a tight, light-resistant container to protect from light and moisture.Store at controlled room temperature 20-25C (68-77F). Excursions permitted to 15-30C (59-86F). [See current USP]Dispense in a tight, light-resistant container to protect from light and moisture.Allergenic extracts are supplied with units listed as: Weight/volume (W/V), Protein Nitrogen Units (PNU/ml), Allergy Units (AU/ml) or Bioequivalent Allergy Units (BAU/ml). Sizes:Diagnostic Scratch: 5 ml dropper application vialsDiagnostic Intradermal: 5 ml or 10 ml vials.Therapeutic Allergens: 5 ml, 10 ml, 50 ml multiple dose vials.Allergenic extracts are supplied with units listed as: Weight/volume (W/V), Protein Nitrogen Units (PNU/ml), Allergy Units (AU/ml) or Bioequivalent Allergy Units (BAU/ml). Sizes:Diagnostic Scratch: 5 ml dropper application vialsDiagnostic Intradermal: 5 ml or 10 ml vials.Therapeutic Allergens: 5 ml, 10 ml, 50 ml multiple dose vials.Allergenic extracts are supplied with units listed as: Weight/volume (W/V), Protein Nitrogen Units (PNU/ml), Allergy Units (AU/ml) or Bioequivalent Allergy Units (BAU/ml). Sizes:Diagnostic Scratch: 5 ml dropper application vialsDiagnostic Intradermal: 5 ml or 10 ml vials.Therapeutic Allergens: 5 ml, 10 ml, 50 ml multiple dose vials.Allergenic extracts are supplied with units listed as: Weight/volume (W/V), Protein Nitrogen Units (PNU/ml), Allergy Units (AU/ml) or Bioequivalent Allergy Units (BAU/ml). Sizes:Diagnostic Scratch: 5 ml dropper application vialsDiagnostic Intradermal: 5 ml or 10 ml vials.Therapeutic Allergens: 5 ml, 10 ml, 50 ml multiple dose vials.Allergenic extracts are supplied with units listed as: Weight/volume (W/V), Protein Nitrogen Units (PNU/ml), Allergy Units (AU/ml) or Bioequivalent Allergy Units (BAU/ml). Sizes:Diagnostic Scratch: 5 ml dropper application vialsDiagnostic Intradermal: 5 ml or 10 ml vials.Therapeutic Allergens: 5 ml, 10 ml, 50 ml multiple dose vials.

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Clinical Information

Chemical Structure

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Clinical Pharmacology

Non-Clinical Toxicology

The hypoglycemic action of sulfonylureas may be potentiated by certain drugs including nonsteroidal anti-inflammatory agents and other drugs that are highly protein bound, salicylates, sulfonamides, chloramphenicol, probenecid, coumarins, monoamine oxidase inhibitors, and beta-adrenergic blocking agents. When such drugs are administered to a patient receiving glipizide, the patient should be observed closely for hypoglycemia. When such drugs are withdrawn from a patient receiving glipizide, the patient should be observed closely for loss of controlbinding studies with human serum proteins indicate that glipizide binds differently than tolbutamide and does not interact with salicylate or dicumarol. However, caution must be exercised in extrapolating these findings to the clinical situation and in the use of glipizide with these drugs.

Certain drugs tend to produce hyperglycemia and may lead to loss of control. These drugs include the thiazides and other diuretics, corticosteroids, phenothiazines, thyroid products, estrogens, oral contraceptives, phenytoin, nicotinic acid, sympathomimetics, calcium channel blocking drugs, and isoniazid. When such drugs are administered to a patient receiving glipizide, the patient should be closely observed for loss of control. When such drugs are withdrawn from a patient receiving glipizide, the patient should be observed closely for hypoglycemia.

A potential interaction between oral miconazole and oral hypoglycemic agents leading to severe hypoglycemia has been reported. Whether this interaction also occurs with the intravenous, topical, or vaginal preparations of miconazole is not known. The effect of concomitant administration of fluconazole and glipizide has been demonstrated in a placebo-controlled crossover study in normal volunteers. All subjects received glipizide alone and following treatment with 100 mg of fluconazole as a single daily oral dose for 7 days. The mean percentage increase in the glipizide AUC after fluconazole administration was 56.9% (range: 35 to 81%).

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WARNINGS: DO NOT SWALLOW

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PRECAUTIONS: FOR PROFESSIONAL USE ONLY

ADVERSE REACTIONS:

Developing teeth of children under age 6 may become permanently discolored if excessive amounts are repeatedly swallowed. The following adverse reactions are possible in individuals hypersensitive to fluoride: eczema, atopic dermatitis, urticaria, gastric distress, headache and weakness.

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Review

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72

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Interactions

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